US4439231A - Preparation of acicular ferromagnetic metal particles consisting essentially of iron - Google Patents
Preparation of acicular ferromagnetic metal particles consisting essentially of iron Download PDFInfo
- Publication number
- US4439231A US4439231A US06/518,000 US51800083A US4439231A US 4439231 A US4439231 A US 4439231A US 51800083 A US51800083 A US 51800083A US 4439231 A US4439231 A US 4439231A
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- United States
- Prior art keywords
- iron
- iii
- feooh
- oxide
- metal particles
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Classifications
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
- H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
- H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
- H01F1/032—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials
- H01F1/04—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials metals or alloys
- H01F1/06—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials metals or alloys in the form of particles, e.g. powder
- H01F1/065—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials metals or alloys in the form of particles, e.g. powder obtained by a reduction
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F9/00—Making metallic powder or suspensions thereof
- B22F9/16—Making metallic powder or suspensions thereof using chemical processes
- B22F9/18—Making metallic powder or suspensions thereof using chemical processes with reduction of metal compounds
- B22F9/20—Making metallic powder or suspensions thereof using chemical processes with reduction of metal compounds starting from solid metal compounds
- B22F9/22—Making metallic powder or suspensions thereof using chemical processes with reduction of metal compounds starting from solid metal compounds using gaseous reductors
Definitions
- the present invention relates to a process for the preparation of acicular ferromagnetic metal particles consisting essentially of iron by reducing acicular iron(III) oxide hydroxide provided with a shape-stabilizing surface coating, or the iron(III) oxide obtained therefrom by dehydration, by means of a decomposable organic compound and hydrogen.
- acicular ferromagnetic metal particles are particularly useful for the production of magnetic recording media.
- iron particles can be prepared by reducing finely divided acicular iron compounds, for example the oxides, with hydrogen or another gaseous reducing agent. For the reduction to take place at a velocity which is industrially acceptable, it has to be carried out at above 300° C. However, this is attended by the problem of sintering of the metal particles that are formed, as a result of which the particles no longer have the shape necessary for achieving the requisite magnetic properties.
- acicular ferromagnetic metal particles consisting essentially of iron can be obtained by reducing acicular iron(III) oxide hydroxide provided with a shape-stabilizing surface coating, or the iron(III) oxide obtained therefrom by dehydration, if the reduction is carried out with a decomposable organic compound and hydrogen at from 270° to 450° C.
- the iron(III) oxide hydroxide or iron(III) oxide provided with a surface coating is reduced with a decomposable organic compound in an inert gas atmosphere at from 270° to 650° C. to FeO x , where x is from 1.33 to 1.44, and, in a second stage, this product is reduced with hydrogen at from 270° to 450° C. to the metal.
- a suitable starting material for the novel process is an iron(III) oxide hydroxide in the form of a mixture of 80-100% of ⁇ -FeOOH and 0-20% of ⁇ -FeOOH, or of 70-100% of ⁇ -FeOOH and 0-30% of ⁇ -FeOOH.
- the appropriate iron(III) oxide hydroxides advantageously have a BET surface area of not less than 20 and not more than 120 m 2 /g, a mean particle length of from 0.10 to 1.5 ⁇ m and a length/width ratio of not less than 5:1, advantageously from 8 to 40:1.
- the iron(III) oxides obtained by dehydrating the said iron(III) oxide hydroxides at above 250° C. are equally suitable.
- metal particles which in addition to iron contain other alloy components, such as cobalt, nickel and/or chromium iron oxides appropriately modified in a conventional manner are employed as starting materials.
- iron(III) oxide hydroxides or iron(III) oxides are then provided in a conventional manner with a shape-stabilizing surface coating which helps to retain the particle shape during the further conversion steps.
- a suitable method of doing this is, for example, to treat the iron(III) oxide hydroxides or iron(III) oxides with an alkaline earth metal cation and a carboxylic acid or another organic compound which has two or more groups capable of chelate formation with the alkaline earth metal cation.
- Another known method which is described in German Laid-Open Application DOS No. 2,646,348, comprises treating the surfaces of the iron(III) oxide hydroxides or iron(III) oxides, in order to stabilize their shape, with hydrolysis-resistant oxyacids of phosphorus, their salts or esters and aliphatic monobasic or polybasic carboxylic acids.
- Suitable hydrolysis-resistant substances are phosphoric acid, soluble mono-, di- and triphosphates, eg. potassium dihydrogen phosphate, ammonium dihydrogen phosphate, disodium orthophosphate, dilithium orthophosphate, trisodium phosphate and sodium pyrophosphate, and metaphosphates, eg. sodium metaphosphate.
- esters of phosphoric acid with aliphatic monoalcohols of 1 to 6 carbon atoms are employed.
- carboxylic acids are saturated or unsaturated aliphatic carboxylic acids which are of not more than 6 carbon atoms and contain no more than 3 acidic groups, and in which one or more hydrogen atoms of the aliphatic chain may be substituted by hydroxyl or amino.
- Particularly suitable acids are oxydicarboxylic acids and oxytricarboxylic acids, eg. oxalic acid, tartaric acid and citric acid.
- shape-stabilizing treatments suitable for the novel process are the conventional surface coatings with tin compounds (German Patent No. 1,907,691) or with silicates or SiO 2 (Japanese Published Applications Nos. 121,799/77 and 153,198/77).
- the iron(III) oxide hydroxides or iron(III) oxides treated in this manner are then reduced to the metal by means of a decomposable organic compound and hydrogen.
- Suitable organic compounds are all organic substances which are decomposable at from 270° to 650° C. in the presence of iron oxide hydroxides or iron oxides.
- Suitable substances for this purpose therefore include relatively long-chain carboxylic acids and their salts, amides of long-chain carboxylic acids, long-chain alcohols, starch, oils, polyalcohols, waxes, paraffins and polymeric substances, eg. polyethylene.
- a high boiling point or sublimation point is advantageous because this avoids losses of organic substance before the reduction begins.
- the iron(III) oxide hydroxide or iron(III) oxide is mechanically mixed with the solid or liquid organic substance, or is coated with this in a suitable solution or suspension of the substance.
- Shape-stabilization and application of the organic substance can be carried out simultaneously or in succession, for example in an aqueous suspension of the particles.
- the organic compound may also be present during or before growth of the iron(III) oxide hydroxide crystals.
- the organic substance is added as early as the beginning of the FeOOH synthesis, for example before the precipitation of Fe(OH) 2 .
- the organic substance may also be added after nucleation is complete, or during or after the growth stage.
- shape-stabilizing surface coating takes place subsequently in the aqueous suspension of the particles, or after the filter cake has been freed from inorganic salts and suspended in water.
- carbon contents of from 0.5 to 20% by weight, based on FeOOH or Fe 2 O 3 , are sufficient.
- the iron(III) oxide hydroxide or iron(III) oxide provided with the surface coating and with the organic compound is reduced under a stream of hydrogen at from 270° to 450° C.
- the reduction time depends on the size of the batch and the type of reactor used, and is accordingly from 30 minutes to 30 hours.
- the novel process can be carried out as follows: in a first stage, the iron(III) oxide hydroxide or iron(III) oxide provided with a surface coating is reduced with the decomposable organic compound under an inert gas, usually nitrogen, at from 270° to 650° C. to FeO x , where x is from 1.33 to 1.44, and in a second stage, carried out directly after the first, the FeO x is then reduced with hydrogen at from 270° to 450° C. to the metal.
- an inert gas usually nitrogen
- the reductions and where relevant the dehydration of FeOOH to Fe 2 O 3 before and at the beginning of the reduction, can be carried out either batchwise or continuously, for example using a separate reactor for each stage.
- the choice between cocurrent and countercurrent flow for solids and gas or vapor streams depends on the number and type of reactors available, eg. rotary kiln or fluidized-bed reactor, the type of starting material, eg. FeOOH or Fe 2 O 3 , and the reduction method used.
- the organic reduction to FeO x can take place simultaneously to the dehydration of FeOOH and at the same point in the reactor; where a continuous procedure is used, the organic substance is added at a suitable point of the reactor, so that the dehydration to Fe 2 O 3 and the organic reduction to FeO x can take place in one and the same reactor but at different points.
- the acicular ferromagnetic metal particles which consist essentially of iron and are obtainable by the novel process still substantially possess the same shape as the starting materials, have a uniform particle size in spite of the transformation reaction carried out beforehand, and, depending on the starting material, are particularly finely divided. As a result of these characteristics, they possess excellent magnetic properties, such as high coercivity and in particular high remanence.
- the high squareness of the hysteresis loop is an indication of a narrow switching field distribution, which results from the uniform shape.
- Metal particles of this type are very useful as magnetic materials for the production of magnetic recording media. However, these substances are advantageously passivated before being further processed. In the passivation procedure, the metal particles are coated with an oxide layer by controlled oxidation, in order to eliminate the pyrophoric characteristics resulting from the large free surface area of the small particles. This is achieved, for example, by passing an air/nitrogen mixture over the metal powder. Passivation may also be effected by wetting the pigments with an organic solvent in the presence of oxygen, or by means of other conventional oxidation and/or coating methods.
- the metal particles obtainable by the novel process are particularly easy to orient magnetically. Moreover, important electroacoustic properties, such as the maximum output levels at long and short wavelengths and, as a result of the finely divided nature of the material, in particular the signal-to-noise ratio are improved.
- the coercive force H c is given kA/m
- the specific remanence (M r / ⁇ ) and specific saturation magnetization (M m / ⁇ ) are each given in nTm 3 /g.
- the specific surface area (S N .sbsb.2) of the pigment was determined by the BET method (N 2 adsorption) and is given in m 2 /g.
- sample 1 Samples of this material, each comprising 5 parts, were mixed with 2.5% by weight (sample 1) and 5% by weight (sample 2) of stearic acid, and the mixtures were reduced in a stream of hydrogen at 350° C. for 8 hours in a rotary kiln.
- the resulting metal particles had the properties shown in Table 1.
- Example 1 The procedure described in Example 1 was followed, except that the FeOOH treated with oxalic acid/phosphoric acid was reduced with hydrogen at 350° C. for 8 hours, in the absence of stearic acid.
- the properties are shown in Table 1.
- samples of this product were dry-blended with 2.5% by weight (sample 1) and 5.0% by weight (sample 2) of stearic acid. Thereafter, samples 1 and 2 were each reduced to the pyrophoric metal pigment (py) in a stream of hydrogen of 30 liters (S.T.P.)/hour. The magnetic properties of the pigments were measured, after which the remainder of each sample was passivated (pa) in a stream of 2 liters (S.T.P.)/hour of air and 30 liters (S.T.P.)/hour of nitrogen at below 60° C. The results of the measurements are shown in Table 2.
- Example 2 Samples (100 parts each) of the FeOOH starting material employed in Example 2 were mixed directly with 2.5% by weight (sample 1) and 5% by weight (sample 2) of stearic acid, and the mixtures were processed further as described in Example 2. The results of the measurements are shown in Table 2.
- a ⁇ -FeOOH treated with oxalic acid/phosphoric acid as described in Example 3 was reduced directly with hydrogen, as described in that Example.
- the coercive force of the pyrophoric material was 63.1 kA/m.
- a ⁇ -FeOOH having a specific surface area of 30 m 2 /g was provided with a tin oxide coating by neutralizing an acidic SnCl 2 -containing aqueous suspension of the particles, as described in German Published Application DAS No. 1,907,697.
- the amount of tin was 1% by weight, based on FeOOH.
- a further coating comprising 3% by weight of olive oil was produced by adding the latter substance.
- the FeOOH treated in this manner was reduced to the metal at 370° C. in a stream of 30 liters (S.T.P.)/hour of hydrogen for 7 hours.
- S.T.P. 30 liters
- Example 4 The procedure described in Example 4 was followed, except that the material treated with tin oxide/olive oil was first reduced to FeO 1 .33 in a stream of nitrogen at 520° C. in the course of 30 minutes and only thereafter reduced with hydrogen to the metal and passivated, as described in Example 4. The results of the measurements are shown in Table 3.
- Example 6 The procedure described in Example 6 was followed, except that the addition of olive oil was omitted. The results of the measurements are shown in Table 4.
- Example 7 The procedure described in Example 7 was followed, except that the material treated with phosphoric acid/olive oil was first reduced in a stream of nitrogen at 470° C. in the course of 30 minutes to FeO 1 .33, and this was then reduced to the metal, as described above. The results of the measurements are shown in Table 5.
- This FeO 1 .33 which contained 0.36% of PO 4 3- and 0.86% of carbon and had an S N .sbsb.2 of 38.7 m 2 /g, was then reduced to the metal with 8.25 m 3 (S.T.P.)/hour of H 2 at 340° C. in a stirred fixed bed, and the product was stabilized at 40° C. with an N 2 /air mixture.
- S.T.P. 8.25 m 3
- Example 10 The procedure described in Example 10 was followed, except that, instead of adding phosphoric acid/olive oil, a mixture of 761 g of SnCl 2 .2H 2 O and 1.2 kg of olive oil was added to the suspension, and thereafter air was passed through for 2 hours.
- the first stage of the reduction gave FeO 1 .34 containing 1.2% of Sn and 0.13% of carbon, and the reduction to the metal was carried out at 310° C. in a fluidized-bed furnace.
- Table 6 The results of the measurements on a sample stabilized with a nitrogen/air mixture at 40° C. are shown in Table 6.
- the resulting powder had the following properties after magnetization to saturation in a charge capacitor:
- the magnetic properties were measured in a magnetic field of 160 kA/m.
- the reference level-to-weighted noise ratio RG A was measured against the reference tape IEC IV, and the signal-to-print-through ratio K o was determined. The results are shown in Table 8.
- Example 15 The procedure described in Example 15 was followed, except that the metal particles obtained as described in Example 10 were employed. The results are shown in Table 8.
- Example 15 The procedure described in Example 15 was followed, except that the metal particles obtained as described in Example 11 were employed. The results are shown in Table 8.
- Example 15 The procedure described in Example 15 was followed, except that the metal particles obtained as described in Example 12 were employed. The results are shown in Table 8.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Hard Magnetic Materials (AREA)
- Compounds Of Iron (AREA)
- Paints Or Removers (AREA)
- Magnetic Record Carriers (AREA)
Abstract
Description
TABLE 1 ______________________________________ H.sub.c S.sub.N.sbsb.2 c [kA/m] [m.sup.2 /g] [% by weight] ______________________________________ Example 1: Sample 1 65.2 27.3 0.22 Sample 2 66.6 30.5 0.29 Comparative Experiment 1 61.4 21.0 0.1 ______________________________________
TABLE 2 ______________________________________ H.sub.c M.sub.r /ρ M.sub.m /ρ S.sub.N.sbsb.2 [kA/m] [nTm.sup.3 /g] [nTm.sup.3 /g] [m.sup.2 /g] ______________________________________ Example 2 Sample 1 (py) 73.3 82 137 Sample 1 (pa) 74 65 111 25.6 Sample 2 (py) 69 91 147 Sample 2 (pa) 75.4 62 107 27.2 Comparative Experiment 2 Sample 1 (py) 62.7 90 149 13.7 Sample 2 (py) 50.7 91 157 ______________________________________
______________________________________ H.sub.c M.sub.m /ρ S.sub.N.sbsb.2 [kA/m] [nTm.sup.3 /g] [m.sup.2 /g] ______________________________________ Example 4 (py) 65.0 89 23.8 Example 4 (pa) 69.5 70 Example 5 (py) 68.4 90 28.5 Example 5 (pa) 75.7 65 ______________________________________
TABLE 4 ______________________________________ H.sub.c M.sub.m /ρ S.sub.N.sbsb.2 [kA/m] [nTm.sup.3 /g] [m.sup.2 /g] ______________________________________ Example 6 63.2 80 29.6 Comparative Experiment 4 62.4 76 21.8 ______________________________________
TABLE 5 ______________________________________ 160 kA/m After saturation S.sub.N.sbsb.2 M.sub.m /ρ M.sub.r /ρ H.sub.c [m.sup.2 /g] ______________________________________ Example 7 166 95 61.1 30.9 Example 8 144 96 70.5 42.2 ______________________________________
TABLE 6 ______________________________________ After saturation S.sub.N.sbsb.2 H.sub.c M.sub.r /ρ [m.sup.2 /g] ______________________________________ Example 10 87.7 88 25 Example 11 90.2 90 23.3 ______________________________________
H.sub.c =87.3[kA/m] and M.sub.r /ρ=61[nTm.sup.3 /g].
______________________________________ S.sub.N.sbsb.2 of the Time Temperature dehydrated product Sample [hours] [°C.] [m.sup.2 /g] ______________________________________ B 1 7 250 99.2 B 2 1 500 44.0 B 3 1 700 25.2 ______________________________________
TABLE 7 ______________________________________ H.sub.c S.sub.N.sbsb.2 Sample kA/m m.sup.2 /g ______________________________________ B 1 89.1 31.9 B 2 85.6 30.4 B 3 90.4 23.5 ______________________________________
TABLE 8 ______________________________________ Example Example Example Example 15 16 17 18 ______________________________________ H.sub.c 78.6 80.9 83.8 90.0 M.sub.r 252 220 221 239 M.sub.m 315 301 305 341 R.sub.f 2.4 1.8 1.9 1.5 Reference +0.6 +2.1 +1.6 +0.4 level-to-weighted noise ratio RG.sub.A Signal- 54.0 56.0 55.5 57.0 to-print- through ratio K.sub.o ______________________________________
Claims (2)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19823228669 DE3228669A1 (en) | 1982-07-31 | 1982-07-31 | METHOD FOR PRODUCING NEEDLE-SHAPED FERROMAGNETIC METAL PARTICLES, ESSENTIALLY IRON |
DE3228669 | 1982-07-31 |
Publications (1)
Publication Number | Publication Date |
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US4439231A true US4439231A (en) | 1984-03-27 |
Family
ID=6169825
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US06/518,000 Expired - Lifetime US4439231A (en) | 1982-07-31 | 1983-07-28 | Preparation of acicular ferromagnetic metal particles consisting essentially of iron |
Country Status (4)
Country | Link |
---|---|
US (1) | US4439231A (en) |
EP (1) | EP0105110B1 (en) |
JP (1) | JPS5944809A (en) |
DE (2) | DE3228669A1 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4576635A (en) * | 1984-02-27 | 1986-03-18 | Fuji Photo Film Co., Ltd. | Process for producing ferromagnetic metal powder |
US4729785A (en) * | 1985-05-10 | 1988-03-08 | Basf Aktiengesellschaft | Preparation of acicular ferromagnetic metal particles consisting essentially of iron |
AU675453B2 (en) * | 1992-09-30 | 1997-02-06 | Canada Conveyor Belt Co., Ltd. | Apparatus and method of damage detection for magnetically permeable members |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6161405A (en) * | 1984-08-31 | 1986-03-29 | Sony Corp | Manufacture of magnetic metal powder |
JPS6161404A (en) * | 1984-08-31 | 1986-03-29 | Sony Corp | Manufacture of magnetic metal powder |
JPS61154013A (en) * | 1984-12-27 | 1986-07-12 | Mitsui Toatsu Chem Inc | Manufacture of needle iron fine particle for magnetic recording |
JPS61126628U (en) * | 1985-01-28 | 1986-08-08 | ||
JP2843124B2 (en) * | 1990-07-02 | 1999-01-06 | 花王株式会社 | Method for producing metal magnetic powder |
DE102010061495A1 (en) * | 2010-12-22 | 2012-06-28 | Bundesanstalt für Materialforschung und -Prüfung (BAM) | Carbothermal reduction of metal oxide involves heating carbothermal reaction of carbonyl compound, organic carbonyl compound, carboxylic acid and/or carboxylate, and releasing carbon monoxide |
Citations (8)
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DE1907691A1 (en) * | 1968-03-05 | 1969-09-25 | Philips Nv | A method of producing a magnetically stable powder for magnetic recording consisting essentially of iron |
DE2014500A1 (en) * | 1969-04-08 | 1970-12-10 | N.V. Philips* Gloeilampenfabrieken, Eindhoven (Niederlande) | A method for producing a magnetically stable metal powder for magnetic recording consisting essentially of iron |
DE1592398A1 (en) * | 1967-02-08 | 1970-12-17 | Bayer Ag | Use of highly coercive needle-like gamma-Fe2O3 for the production of magnetogram carriers |
DE2436096A1 (en) * | 1973-10-23 | 1975-04-24 | Crompton & Knowles Corp | METHOD AND SYSTEM FOR THE PRODUCTION OF MIXED, SPINNABLE FIBER MATERIALS |
DE2434058A1 (en) * | 1974-07-16 | 1976-02-05 | Basf Ag | Process for the production of needle-shaped, ferrous ferromagnetic metal pigments |
JPS51121799A (en) * | 1975-04-18 | 1976-10-25 | Fujitsu Ltd | Manufacturing method of electlet and piezoeiectric material |
DE2646348A1 (en) * | 1976-10-14 | 1978-04-20 | Basf Ag | FERROMAGNETIC METAL PARTS CONSISTING MAINLY OF IRON AND THE PROCESS FOR THEIR PRODUCTION |
DE2714588A1 (en) * | 1977-04-01 | 1978-10-12 | Basf Ag | PROCESS FOR THE PRODUCTION OF NEEDLE-SHAPED FERROMAGNETIC IRON PARTS |
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JPS52122213A (en) * | 1976-04-05 | 1977-10-14 | Hitachi Ltd | Production of ferromagnetic metal powder |
JPS52144400A (en) * | 1976-05-27 | 1977-12-01 | Toda Kogyo Corp | Process for preparing magnetic ironoxide particle for magnetic recording material |
DE2731845A1 (en) * | 1977-07-14 | 1979-01-25 | Devender Dr Ing Dhingra | Metal powder prodn. in a rotary kiln - by reducing oxide starting material which contains an added organic substance |
DE2743298A1 (en) * | 1977-09-27 | 1979-04-05 | Basf Ag | FERROMAGNETIC METAL PARTS CONSISTING MAINLY OF IRON AND THE PROCESS FOR THEIR PRODUCTION |
JPS5573803A (en) * | 1978-11-25 | 1980-06-03 | Hitachi Maxell Ltd | Production of magnetic alloy powder |
DE2935358A1 (en) * | 1979-09-01 | 1981-03-26 | Basf Ag, 67063 Ludwigshafen | METHOD FOR PRODUCING NEEDLE-SHAPED FERROMAGNETIC IRON PARTICLES AND THE USE THEREOF |
JPS5946282B2 (en) * | 1979-12-11 | 1984-11-12 | 戸田工業株式会社 | Method for manufacturing metallic iron or alloy magnetic particle powder mainly composed of iron |
JPS5754205A (en) * | 1980-09-17 | 1982-03-31 | Hitachi Maxell Ltd | Preparation of magnetic powder |
-
1982
- 1982-07-31 DE DE19823228669 patent/DE3228669A1/en not_active Withdrawn
-
1983
- 1983-07-23 EP EP83107240A patent/EP0105110B1/en not_active Expired
- 1983-07-23 DE DE8383107240T patent/DE3374480D1/en not_active Expired
- 1983-07-28 US US06/518,000 patent/US4439231A/en not_active Expired - Lifetime
- 1983-08-01 JP JP58139512A patent/JPS5944809A/en active Granted
Patent Citations (11)
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DE1592398A1 (en) * | 1967-02-08 | 1970-12-17 | Bayer Ag | Use of highly coercive needle-like gamma-Fe2O3 for the production of magnetogram carriers |
DE1907691A1 (en) * | 1968-03-05 | 1969-09-25 | Philips Nv | A method of producing a magnetically stable powder for magnetic recording consisting essentially of iron |
DE2014500A1 (en) * | 1969-04-08 | 1970-12-10 | N.V. Philips* Gloeilampenfabrieken, Eindhoven (Niederlande) | A method for producing a magnetically stable metal powder for magnetic recording consisting essentially of iron |
DE2436096A1 (en) * | 1973-10-23 | 1975-04-24 | Crompton & Knowles Corp | METHOD AND SYSTEM FOR THE PRODUCTION OF MIXED, SPINNABLE FIBER MATERIALS |
DE2434058A1 (en) * | 1974-07-16 | 1976-02-05 | Basf Ag | Process for the production of needle-shaped, ferrous ferromagnetic metal pigments |
US4017303A (en) * | 1974-07-16 | 1977-04-12 | Basf Aktiengesellschaft | Manufacture of acicular ferromagnetic metal pigments containing iron |
JPS51121799A (en) * | 1975-04-18 | 1976-10-25 | Fujitsu Ltd | Manufacturing method of electlet and piezoeiectric material |
DE2646348A1 (en) * | 1976-10-14 | 1978-04-20 | Basf Ag | FERROMAGNETIC METAL PARTS CONSISTING MAINLY OF IRON AND THE PROCESS FOR THEIR PRODUCTION |
US4155748A (en) * | 1976-10-14 | 1979-05-22 | Basf Aktiengesellschaft | Manufacture of ferromagnetic metal particles consisting essentially of iron |
DE2714588A1 (en) * | 1977-04-01 | 1978-10-12 | Basf Ag | PROCESS FOR THE PRODUCTION OF NEEDLE-SHAPED FERROMAGNETIC IRON PARTS |
US4178171A (en) * | 1977-04-01 | 1979-12-11 | Basf Aktiengesellschaft | Manufacture of acicular ferromagnetic iron particles |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4576635A (en) * | 1984-02-27 | 1986-03-18 | Fuji Photo Film Co., Ltd. | Process for producing ferromagnetic metal powder |
US4729785A (en) * | 1985-05-10 | 1988-03-08 | Basf Aktiengesellschaft | Preparation of acicular ferromagnetic metal particles consisting essentially of iron |
AU675453B2 (en) * | 1992-09-30 | 1997-02-06 | Canada Conveyor Belt Co., Ltd. | Apparatus and method of damage detection for magnetically permeable members |
Also Published As
Publication number | Publication date |
---|---|
DE3374480D1 (en) | 1987-12-17 |
DE3228669A1 (en) | 1984-02-02 |
EP0105110A3 (en) | 1985-11-21 |
EP0105110A2 (en) | 1984-04-11 |
EP0105110B1 (en) | 1987-11-11 |
JPS5944809A (en) | 1984-03-13 |
JPH0475641B2 (en) | 1992-12-01 |
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